Issue 18, 2024

Nickel-catalyzed reductive cross-coupling of monofluoroalkyl triflates with aryl halides for monofluoroalkylated arenes

Abstract

Here, we report a nickel-catalyzed reductive C(sp3)–C(sp2) cross-coupling of monofluoroalkyl triflates with aryl halides, yielding a series of functionalized monofluoroalkylated arenes. This method is characterized by mild reaction conditions, a broad substrate scope, with excellent functional group compatibility. Facile follow-up transformations highlight its utility as an appealing tool in the synthesis of pharmaceutical derivatives.

Graphical abstract: Nickel-catalyzed reductive cross-coupling of monofluoroalkyl triflates with aryl halides for monofluoroalkylated arenes

Supplementary files

Article information

Article type
Research Article
Submitted
07 Jun 2024
Accepted
13 Jul 2024
First published
16 Jul 2024

Org. Chem. Front., 2024,11, 5010-5015

Nickel-catalyzed reductive cross-coupling of monofluoroalkyl triflates with aryl halides for monofluoroalkylated arenes

Z. Li, H. Peng, P. Zhang, Y. Hu, C. Pi, C. Zhu and H. Xu, Org. Chem. Front., 2024, 11, 5010 DOI: 10.1039/D4QO01033G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements